rs4656940
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4656940(A;A) |
| Make rs4656940(A;G) |
| Make rs4656940(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 160860478 |
| Gene | CD244 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4656940 |
| dbSNP (classic) | rs4656940 |
| ClinGen | rs4656940 |
| ebi | rs4656940 |
| HLI | rs4656940 |
| Exac | rs4656940 |
| Gnomad | rs4656940 |
| Varsome | rs4656940 |
| LitVar | rs4656940 |
| Map | rs4656940 |
| PheGenI | rs4656940 |
| Biobank | rs4656940 |
| 1000 genomes | rs4656940 |
| hgdp | rs4656940 |
| ensembl | rs4656940 |
| geneview | rs4656940 |
| scholar | rs4656940 |
| rs4656940 | |
| pharmgkb | rs4656940 |
| gwascentral | rs4656940 |
| openSNP | rs4656940 |
| 23andMe | rs4656940 |
| SNPshot | rs4656940 |
| SNPdbe | rs4656940 |
| MSV3d | rs4656940 |
| GWAS Ctlg | rs4656940 |
| GMAF | 0.2911 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21102463 ]
|
| Trait | Crohn's disease |
| Title | Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. |
| Risk Allele | A |
| P-val | 6E-7 |
| Odds Ratio | 1.15 [1.09-1.21] |
